UNLV Retrospective Theses & Dissertations
1-1-1999
The disability press: A wheel still in spin
Cindy Schwartz McCoy University of Nevada, Las Vegas
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Repository Citation McCoy, Cindy Schwartz, "The disability press: A wheel still in spin" (1999). UNLV Retrospective Theses & Dissertations. 1027. http://dx.doi.org/10.25669/g7xz-k2ur
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Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. THE DISABILITY PRESS: A WHEEL STILL IN SPIN
by
Cindy Schwartz McCoy
Bachelor of Arts The University of the State of New York 1990
Master of Arts The University of Santa Monica 1990
A thesis submitted in partial fulfillment of the requirements for the
Master of Arts Degree Hank Greenspun Department of Communication Studies Greenspun College of Urban Affairs
Graduate College University of Nevada, Las Vegas August 1999
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Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Copyright by Cindy Schwartz McCoy 1999 All Rights Reserved
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Thesis Approval UNIV The Graduate College University of Nevada, Las Vegas
July 27 19 99
The Thesis prepared by
Cindy Schwartz McCoy
Entitled
The Disability Press; A Wheel Still in Spl]
is approved in partial fulfillment of the requirements for the degree of
Master of Arts in Communication ______
Examination Committee Chair
Dean of the Graduate College
Examination CommilSée iber
Examinanon Committee Mtter
Graduate College Faculty Representative
11
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. ABSTRACT
The Disability Press: A Wheel Still in Spin
by
Cindy Schwartz McCoy
Dr. Richard Jensen, Examination Committee Chair Professor of Communication University of Nevada, Las Vegas
This study, exploring the messages of the disability press, also utilizes Marxist theory to
explain empowerment in the disability community. Although Marxism has significant
value for explaining disability oppression, Marx’s theory of internal relations, describing an
interconnected web of organizational structure and the accompanying relationships, sheds
light on the political nature of disability empowerment. A world view characterized by an
economic base and social superstructure models an intrinsically enmeshed impairment base
and social superstructure model of disability. The covers and cover stories of Mouth.
Mainstream. Ragged Edge, and New Mobility magazines are catalogued and a
representative sample is analyzed in order to demonstrate the political nature of the
disability community’s empowerment.
m
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ABSTRACT...... üi
TABLE OF CONTENTS ...... iv
ACKNOWLEDGMENTS...... v
CHAPTER I INTRODUCTION ...... 1 The Disability Press and Empowerment...... 1
CHAPTER II A DISABILITY HISTORY ...... 13 A History of Disability Oppression...... 13
CHAPTER III METHODOLOGY...... 28
CHAPTER IV ANALYSIS ...... 42 The Messages ...... 45 Summary...... 51 Conclusion...... 56
CHAPTER V CONCLUSIONS AND FUTURE STUDY...... 59 Political Awareness...... 59
BIBLIOGRAPHY...... 68
VITA ...... 74
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Thanks to my examining committee, especially Dr. Richard Jensen
Thanks to my listeners
And my angels
To Dr. Richard Visone. who reminded me just to write while the rest of my world did
whatever
To Mishu
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INTRODUCTION
The Disability Press And Empowerment
Alternative methods of communicating about disability have been necessary since
the passage of the1990 Americans With Disabilities Act (Mitchell & Snyder, 19967, p. 12).
Mainstream structures responsible for the portrayal of disability are slowly but surely
changing (Clogçton, 1992 & Haller, 1995). “(I)nterest in the social and political
dimensions of disablement has intensified considerably both at the general level and in
universities and academic institutions” ( Bames, 1997, p.l). Additionally, “with the rise in
people’s consciousness, a disability culture, based on shared experience, has emerged”
(Iwakuma, 1997). Stephen Brown names some of the many grass roots movements, the
disability press, analytical academic organizations, and artistic endeavors as the tip of the
Disability Culture Movement (Brown, 1998, p.l). Lathrop (1995) recognizes the role of
the disability press:
Like other minority communities did in the past, the disability community has
begun to build upon common ground through the written word—through
publications such as Mouth. Mainstream, the Disabilitv Rag, and New Mobility, as
well as in the national and local levels—reporting news, providing role models,
exploring important issues, and covering the concerns of the community (p.35).
1
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Stereotypical images have served as the primary public locus for disability
identification (Shapiro, 1995). While mainstream culture used negative images to define
the subjects and circumstances of disability, individuals with disabilities internalized the
images, invalidating their own human experiences (Charlton, 1998). Movie screen images
and literary characters have taken predictable forms that comprise ableism (Nelson, 1997).
Ableism is that set of often contradictory stereotypes about people with disabilities
that acts as a barrier to keep them from achieving their full potential as equal
citizens in society. Among these are the beliefe that people with disabilities are
inherently able to manage their own lives, that they are embittered and malevolent,
and that they are, by reason of their disability, morally, intellectually, and spiritually
inferior to temporarily able-bodied people, or, conversely, that people with
disabilities are saintlike, ever cheerful, asexual, childlike, and unusually heroic.
Ultimately, it is the belief that people with disabilities are different from “normal”
people, and that their lives are inherently less worthwhile than those of people
without disabilities. (Pelka, 1997, p.3)
Today, disabled journalists, poets, and story tellers are
expanding the array of options from which to imagine the lives of people with
disabilities. Such first person narratives provide readers with an alternative
perspective on what it is to live with a disability.. . . Autobiographical narratives
demand that the disabled subject develop a voice that privileges the agency of a
bona fide perspective of disability (Mitchell & Snyder, 1997 p. 10).
Chapter two details disability history, historical images, and autobiographical narrative.
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Beginning with historical images of disability, this study addresses changes
occurring in perceptions of the disability experience. The disability press and discourses of
disability construction demonstrate how the disability community is transforming from an
ignored and silent body to an empowered constituency. Then, drawing on Marxism as a
foundation for understanding disability oppression and as the social structure for
explaining its empowerment, an analysis of of Mouth. Ragged Edge. New Mobility, and
Mainstream magazine article and cover pages provide clues to a subculture’s definitions of
reality. In some cases, foundational studies are included in the introduction, more are
included in later chapters. This study builds on the dissertation of Ransom (1997). The
abstract for Ransom’s study states that
very few scholars have studied media produced by and for people with disabilities.
This dissertation is one of the first attempts to do so, and to analyze how these
publications may help forge group identity. The study examines the tensions of
liberal-pluralism and Marxist theories and their ability to explain the function of
disability publications in American society. The researcher explored disability
publication editors’ perceptions about disability related issues, and examines how
disability related publications are similar to feminist and African American
publications (Ransom, 1997).
The Disabilitv Press
The disability press, gaining popularity after the passage of the Americans with
Disabilities Act in 1990, captures and perpetuates the sentiments of an entire community,
proposes Douglas Lathrop, as he details founding philosophies of New Mobility. Mouth.
Mainstream, and the Disabilitv Rag. In “Challenging Perceptions,” published in the
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literary journal. The Quill. Lathrop (1995) recognizes the existence of shared
commonalties and polarities within the community. He discusses the case of Ellen Stohl
and Lucy G win, two women, both with disabilities, both dedicated to changing
stereotypes, but with opposing views and tactics. Stohl, challenging the idea that disabled
equals ugly, appeared in a Plavbov pictorial with wheelchair flaunted. Gwin rages against
the idea that people with disabilities must be sugar-coated and prettified before they
experience media exposure (p. 36). Both express views that stray fi-om popular images,
even though they seem to conflict.
The magazines, all offering alternatives to prevailing images, are contextually and
editorially diverse. Lathrop (1995) presents the commonality of people telling their own
stories and coming to see themselves as part of a group with common civil-rights
struggles as evidence that a community exists. He recognizes that all the intracommunity
publications want to tell the real story—not the routinely used tear-jerker or inspirational
parable. But each is singular in its philosophical mission. Lathrop points out that New
Mobüitv magazine wants to present readers with images of disabled people leading
independent and active lives. Lathrop reports New Mobility editor Barry Corbet’s belief
that by presenting images that are positive but not patronizing, the magazine increases the
public profile of the disability community.
Lathrop (1995) goes on to say that conversely. Mouth magazine is committed to
the coverage of the disability-rights movement with a militant, in-your-face attitude. It
proclaims the disability movement as the most recent civil rights movement and demands
that the nondisabled see past their pity. The Disabilitv Rag, states its mission, Lathrop
says, as analysis of the roots of discrimination and disenfi-anchisement. Maintaining a
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dedication to civil rights, it shows the consumer’s, the professional’s and the radical’s side
of the experience. The author finally reports that Mainstream magazine is one of the
community’s moderate voices covering current issues and lifestyle/culture features.
The Social Model
In 1980, The World Health Organization (WHO) developed the International
Classification of Impairments, Disabilities and Handicaps (ICIDH) which intended to
provide a global fi'ame of reference for understanding disability. In the ICIDH scheme, the
word “impairment” describes functional deficits and the term “disability” refers to any
interference with personal activities. The term “handicap” conceptualizes any hindrances
imposed by society on the individual because of the impairment. The various models
proposed to explain and classify disablements may be expressed in a dialectic of the
“medical model” vs. the “social model”. The medical model views the disablement
phenomenon as a “personal” problem, “giving paramount importance to the physiological
features of illness and impairment, including certain expectations of medical care”
(Lonsdale, 1990. p. 34). Health care is viewed as the main issue and at the political level it
is health care policy that is of primary importance. The social model of disablement, on the
other hand, “regards disability as a complex of constraints that the able-bodied population
imposes on the behavior of... impaired people” (Liachowitz, 1988, p. 1). Disablement is
not an attribute of the person, but a complex collection of conditions, many of which are
created by the societal environment. Hence the management of the problem requires social
action and it is the collective responsibility of society to make the environmental
modifications necessary for the full participation of people with disabilities into all areas of
social life. The issue is, therefore, an attitudinal or ideological one which requires social
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change, while at political level it is a question of human rights (World Health
Organization, 1997). The social construction of disability assumes that barriers to fuU
inclusion He in society and not in the individual. The implications and repercussions of that
consciousness shift have been addressed by many in various disciplines and formats.
Electronic communication provides information about community politics,
philosophy, psychology, and fantasies. There are advocacy listservs like Justice For All
and the one ADAPT disseminates. There are chat lines like the one hosted by New
Mobility, with no moderation or registration process required. There are moderated lists
hosting conversation threads about any and all subjects but with a ibcus on specific
disability issues such as spinal cord injury, mobility, physical/sexual abuse, attendant care.
Academic lists, like Disability-Dialogues and Disability-Research, both originating at the
University of Leeds in the United Kingdom, but attended globally, provide an arena for a
broad range of subjects. One recent discussion explored definitions of the disability
community.
The debate rages as to the ethnicity of disability, who is included, the purposes of
community and the relationship of the disabled community to mainstream culture. British
scholar Ayesha Vernon explores the issue of commonality and difference in the disabled
people’s movement in the archived version of this Leeds conference presentation. She
recognizes that the oppression of disability is complicated by additional “otherness” of
gender, race, sexuality, class, and age but claims that the push for eradicating disability
(the social stigma and political barriers of impairment) must be a war against all prejudicial
action. She summarizes by questioning if the disability movement would be well served by
forming an alliance with other groups fighting oppression (Vemon, 1997).
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Marxism And Disabilitv
James Charlton’s Nothing About Us Without Us understands the dimensions of
enforced oppression through Marxist principles of hegemony, false consciousness and
alienation. He recognizes that “(t)he oppression of 500 million people with disabilities is
rooted in the political-economic and cultural dimensions of everyday life” ( 1998, p.20).
Calling his book “part descriptive, part conversational, part theoretical, and wholly
argumentative” Charlton “synthesizes theories and opinions about oppression and
exploitation, power and ideology, resistance and empowerment” (p.20). The author’s
threefold mission challenges existing epistemologies and ontologies of disability. Charlton
names Marxist theory as a basis for understanding existing practices and new foundations,
structures and contexts in which to think about the relationships and conditions of
oppression and resistance and to understand and support disability rights.
There are other volumes that include Marxist-Disability discussions. In the article
“Work, Utopia and impairment”, [the author’s capitalization], appearing in Disabilitv &
Societv: emerging issues and insights. Paul Abberly (1996) contends that “(i)n terms of
the analysis of the oppression of disabled people in capitalist societies, Marxism has
provided effective tools, but in relation to Marxist Utopian thought I think we encounter
profound difficulties for impaired people” (p, 68). Michael Oliver (1996), in
Understanding Disabilitv: from theory to practice, suggests that Marxist theory is useful in
approaching disability at an ontological level. He also refers to Marx in discussions of
political economy and empowerment.
Colin Bames (1997) writes that “to appreciate fully the extent and significance of
the oppression of disabled people an understanding of history and its relationship to
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western culture: the central value system around which western society is clustered, is
vital” . The socio-political theory “rooted on the materialist analysis of history associated
with Marx maintains that disability and dependence are the social creation of industrial
capitalism” (1997). Citing Michael Oliver’s The Politics of Disablement. Bames (1997)
points out that the tragic theory of disability, one based on the rise of the institution as a
means of both social provision and control under capitalism resulted in the emergence of
the individual medical approach to disability. This personal tragedy theory of disablement
has, he says, achieved ideological hegemony in that it has become translated into the
emergence of capitalist society (1997).
Methodology
Although the oppression of disability may be understood through Marxist theories
of economic, socio-political, and historical aspects, it is the complex relationship between
those aspects that can be used to explain disability empowerment. Because “(s)ocial
formations are a complex hierarchy of functionally organized institutions or instances
whose entity can neither be ignored altogether nor reduced to a single closed system”
(Resch, 1992, p.35) and because “the individual is held to be in some kind of union with
his object; they are relationally contained in one another” (Oilman, 1976, p.28), then the
collective impact of the ADA, the disability press, and empowering narrative is significant
for community formation and empowerment.
The disability press is a useful representation of the disability experience. Marxism
is a useful structure for explaining significant aspects of the disability experience.
Therefore, it follows that Marxian analysis is an appropriate methodology for
understanding the images and text of the disability press as interpretation of the disability
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experience. Although orthodox Marxist theory is concerned with the economic and
institutional analysis of media systems, studies after 1980 have examined media as an
ideological practice. Such critical interpretations employ various analytic methods to
determine the ways in which “a particular text or group of texts functions as part of
ideological practice and offers a system of knowledge or a way of experiencing the world
for a (reader). An ideological criticism of the text and images can “clarify how and why
the medium carries the meanings and values it does for its audience” (White, 1987, p. 142).
This study parallels a 1996 essay from the feminist perspective by Sonia Foss. Like Foss, I
focus on the “process by which (a minority group) comes to see their symbols rituals and
regular practices—the content of their experiences that tends to be overlooked in the
(dominant) world view (Foss, 1996, p. 205). Foss (1996) explains
A prerequisite to having their voices heard in a discursive fonnation or the
dominant culture is that members of a submerged group must develop their own
authentic voice. They must develop knowledge and discourse out of their own
experiences and interpret and label these experiences in their own terms. Perhaps
even more important, they must come to see their experiences as legitimate and
valuable. Developing this authenticity and attributing power are difficult for a
submerged group, however, because their experience has been interpreted for them
for so long by others and devalued by those others. The submerged group has been
trained to see itself as represented in the dominant discourse of the culture and has
come to subordinate even its authentic and potentially powerful voice to that
culture (Schulz, 1984). . . . But empowerment cannot happen without a strong
sense of identity within the submerged group apart from the dominant culture.
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Group members first must possess the “courage to be and to speak . . . the
Courage to Blaspheme” (Daly, 1978) the definitions of themselves as powerless
that have been established by the dominant discourse (1996, p. 206).
Mitchell & Snyde (1997) interpret the mechanisms of misrepresentation for the disability
community:
In discussions of the ways in which disability has been historically represented . .
. disability scholars have also begun to identify working catalogs of disability’s
cultural meanings. Such a catalog reflects ableist projections onto disability, and
consequently, a compilation of these restrictive narrative possibilities reveals the
method by which disability has been colonized . .. ( p. 20)..
Expecting to find an array of blasphemous expressions directed at oppressors, this study
analyzes magazine messages for examples of group identity: self-defined contradictions to
prevailing designations.
It is simplistic to explain the increased visibility of people with disabilities by
crediting federally legislated change. The Americans with Disabilities Act created a
network of rules governing the inclusion and access for people with disabilities into the
culture. Legislation may not explain a community’s growing awareness of personal needs.
In an attempt to more fully understand the phenomenon of disability empowerment, it
makes sense to integrate current thinking about the social construction of disability into
any explanation of that change. If one understands that a large part of the problem of
impairment, the handicap, originates in social structure, then one naturally begins to search
for keys to alleviation there.
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This study examines the cover and cover stories from four popular magazines
representing the disability press. Mouth. Mainstream, and the Disabilitv Rag are cross-
disability publications, Mainstream is written for those with mobility impairments. Mouth
and Disabilitv Rag are grass roots type issues, which are inexpensively printed in black and
white on plain paper, they accept no advertising. Mainstream and Mainstream are glossy,
frill-color magazines with advertisements appropriate to the readership. The latter issues
send complimentary copies to professional offices, the former are available by subscription
only. Although the publications all address the disability experience from an insider’s
vantage point, this study anticipates finding as many differences as similarities between the
issues that accept advertising and those that do not. The similarities may be analyzed to
tell the story of a group’s empowerment, publishing messages that contradict the
dominant culture’s excluding beliefe and practices.
Every attempt to study the disability community, from strength to weakness, and
all in between, is an attempt to understand a feared, stigmatized, and ignored state of
being. Mitchell and Snyder (1997) assert that a ‘Sosible increase in the number of scholars
with disabilities would radically affect the ways in which we imagine this constituency’s
relationship within and to social institutions” (p. 2). Beyond that, it is an attempt to
understand our culture and the human nature that drives it. Theresa Thompson, a pioneer
in the field of disability communication, documents a 12 year journey to find a home for
her research. Beginning in the early seventies, she found studies matching her own
disability communications interests in psychology journals, special education studies, the
field of sociology, especially the work of Erving Gofifinan, and health communications.
Thompson refers to the first journal that exclusively covered disability issues, Disabilitv
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Studies Quarterly, which appeared in 1980, and filled a large gap in scholarly
communications about disabilities studies. Thompson hails the creation of the Caucus on
Communication and Disability, part of the National Communication Association, as an
appropriate home for her research on communication and disability. Wanting to redefine
how colleges and universities view people with disabilities, several scholars are dedicated
to creating disability studies departments as separate entities.
When Barbara Walters interviewed Tom Hanks for the “Top 10 Interesting People
of 1998”, she asked if he cared that he was considered as having no sex appeal. He told
her that he knew that people said that, and he totally embraced that about himself. That
made him kind of sexy, didn’t she think. As people with disabilities embrace their
differences, the result is strength, empowerment and ability: the new images projected in
the disability press.
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A DISABILITY HISTORY
A History of Disability Oppression
Although recent social changes have had a positive effect for many in the disabled
community, “(t)he vast majority of people with disabilities have always been poor,
powerless, and degraded. Disability oppression is a product of both the past and the
present. . . [it is a] remnant of ancien régimes of politics and economics, customs and
beliefs” (Charlton, 1998, p.21). Capitalism, the primary system of social and economic
exchange in the Western world , “emphasizes the strong economic reasons for the
exclusion of disabled people. It is the embodiment of these social and economic relations
under capitalism which has led directly to the exclusion of disabled people within capitalist
societies” (Oliver. 1990, p. 21). Since contributing “conditions correspond at every stage
to the simultaneous development of the productive forces, their history is at the same time
the history of the evolving productive forces taken over by each generation, and is
therefore the history of the development of the individuals themselves” ( Marx & Engels,
1965, p.72). James Charlton, in Nothing About Us Without Us. presents disability
oppression as a multidimensional characteristic of the disability experience. This chapter
models his format. Disability empowerment, when viewed from a historical perspective.
13
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appears not so much as a reaction of revolutionary structural shifts, but as an evolutionary
process, a cumulative aggregate of subtle and immense changes.
Political and Economic History: Leading to the ADA
There is a tendency to name economic determinants as the primary cause of
disability oppression. “On one level a political economy of disability is easy to establish.
That people with disabilities are powerless and poor is incontestable. Every socioeconomic
indicator says so. Since feudalism and even earlier, they have lived outside the economy
and political process” (Charlton, 1998, p.37). The value of those lives lived outside
normal boundaries has been debated through time. Movements to exterminate, manipulate,
and hide people with disabilities have existed, in some cases simultaneously with
programs to support and subsidize them.
Early twentieth century programs, like the Veterans Bureau and the Social
Security Act, made taking care of the disabled a national responsibility. At the same time,
eugenics, a movement proposing heredity improvement and threatening the existence of
that same population, was receiving media attention. The American eugenics movement
called for forced sterilization of the disabled: “while eugenics claimed to be purely
objective,... subjective values, such as aesthetic standards of beauty and ugliness and
moral attributes of responsibility, were central to eugenic constructions of hereditary
disease and disability” (Pemick, 1997, p. 90).
Beautiful children with disabilities were the tools of charity fund raising telethons
like Jerry Lewis’ Labor Day Show. The use of poster child images capitalized on ableist
sentiments, raising funds and soothing public consciousness. Telethons are recognized as
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demeaning and paternalistic shows which celebrate and encourage pity. .. . Other
problems are that they give the public the idea that everything is taken care of, that
there’s no need to worry about discrimination or civil rights or social services,
because “those people” have “their charities” to take care of them (Pelka, 1997, p.
302).
In recent years, former poster kids and activist groups, including Evan Kemp, Jr. and
Jerry’s Orphans, have mobilized each year to picket the television stations airing the
shows.
The Salk vaccine discovery in 1952 encouraged the public to believe disability and
illness was curable and should be cured. “Disability .. exceeds a culture’s predictive
capacities and effective interventions” (Mitchell & Snyder, 1997, p. 3). GuUt and shame,
natural psychological consequences, are assaults to the ego.
Guilt is the attack of the superego, or conscience, and shame arises from the
opprobrium of others.. . . The sociologist George Herbert Mead wrote that an
individual’s concept of his or her self is a reflection, or, more accurately, a
refraction. As in a fun-house mirror, of the way he or she is treated by others. And
if a person is treated with ridicule, contempt or aversion, then his own ego is
diminished, his dignity and humanity are called into question. . . . Damage to the
body, then, causes diminution of the self, which is further magnified by the
debasement of others (Murphy, p. 92).
Ten years after Salk’s discovery, James Meredith walked into the University of
Mississippi in 1962, and Ed Roberts, the founder of the independent living movement,
rolled into the University of California at Berkeley. Roberts had severe physical
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limitations caused by the polio virus he had contracted when he was 14. He believed he
should be able to attend the university despite his need for an iron lung. By 1967, he and
his cohorts, the “12 Rolling Quads” were a power on the Berkeley campus. In 1970, the
antidropout student program was being run primarily by and for physically disabled
students. The program was funded by the Department of Health, Education, and Welfare
($81,000) and the University of California ($2000). The first Center for Independent
Living opened in March 1972, serving San Francisco. It was nonstudent directed,
supporting a growing population of area residents with disabilities. On the opposite coast,
Judy Heumann, another polio survivor, won a discrimination suit against the New York
School District and began a political action organization, ‘Disabled in Action’ (Shapiro,
1995).
That same year, a precursor to the ADA passed quietly. The Rehabilitation Act of
1972, section 504, “making it illegal for any federal agency, public university, defense or
other federal contractor, or any other institution or activity that received federal funding to
discriminate against anyone ‘solely by reasonof... handicap’ ” (Shapiro, 1994, p. 65)
passed into law.
1974 brought a newly devoted Justin Dart back to the U.S. and the disability rights
cause. Dart, post-polio, having lived a privileged life, spent years in Japan studying
Ghandi’s writing and rehabilitating his soul. He returned to wage a countrywide, politically
educational campaign for people with disabilities. In 1981, Evan Kemp, Jr., presidential
advisor and former poster child, attacked the Muscular Dystrophy Association for its pity
based fund- raising tactics (Shapiro, 1995).
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Active protest became part of the disability empowerment scene in 1978 with a
small but powerful civil rights movement “The beginnings of Americans Disabled for
Attendant Programs Today (ADAPT) can be traced to a small demonstration in
Colorado” (Pelka, p. 123). Using the nonviolent tactics of Martin Luther King’s civil rights
demonstration, ADAPT (at that time signifying American Disabled for Accessible Public
Transit) demanded the availability of accessible buses in Denver. Disabled demonstrators
effectively halted bus service throughout the city by surrounding buses with wheelchairs,
attempting to crawl into the vehicles and occupying administrative offices. Winning a
victory in Denver (a city erected plaque commemorates the event), ADAPT focused on
ensuring passage of civil rights legislation and finally to its current focus on affordable
attendant care programs paid for by a reduction of nursing home funding.
Organized efforts to create support for a single all-inclusive law promising equal
rights for persons with disabilities began as Dart issued a report asking Congress to “act
forthwith to include persons with disabilities in the Civil Rights Act of 1964 and other civil
and voting rights legislation and regulations” (Pelka, 1997, p. 18). Although that effort
failed, the bill was redrafted by the staffs of Senators Edward Kennedy and Thomas
Harkin, with input fi'om a committee of disability rights attorneys, and representatives
from the White House, Department of Justice and Senator Robert Dole. Efforts to gain
support for the bill included organizational lobbying and individual grass roots campaigns.
President George Bush signed the ADA into law on July 26, 1990.
Although passage of the law brought some disillusionment fi"om those impatient to
see an immediate change in societal behavior, the ADA “has made disability rights
a part of the national agenda and has raised people with disabilities to full
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citizenship under the law for the first time in American history” (Pelka, 1997, p.
22).
Cultural Views: Media Images and Narrative
Incomplete public images, misrepresenting and discounting disability are found in
every arena of information dissemination. Ransom (1996) concludes that “a combination
of liberal pluralism and Marxist explanations is a better option for explaining and
predicting the role of media, than either alone” (p.246).
The liberal pluralism theory of media in American society informs us that media is
a marketplace of competing ideas.. . . Liberal pluralists assume that all audience
members/citizens have equal access to media. [They] also assume that our
educational systems, government, and other public institutions are functioning in
such a way that all citizens are equally motivated to express their ideas and
aspirations in media (p. 241)
Marxist theory, contradictorily, describes mass media as the commonly inaccessible tools
of an elite class who benefit fi-om preserving the status quo.
The pages of children’s literature, comic books, classic literature and film, as well
as mainstream media reporting often capture and perpetuate the cultural misunderstanding
and fear of difference. Disability misrepresentations fall into seven categories, contend
Bogdan and Bilkin, called “handicapist stereotypes” (Nelson, 4). Number one, the
disabled person as pitiable and pathetic, exemplifies fund-raising marathons or telethons.
Number two, the disabled person as supercrip, is the image of someone triumphing over
disability and achieving uncommon success. The third plays on “subtle and deeply held
fears” (Nelson, 1994 p. 6). It is the disabled person as evil, sinister, and criminaL
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demonstrated by the villainous characters in Dr. No and Dr. Straneelove. or the one-
armed killer from the Fugitive. (Nelson, 1994 p. 6). Number four, the “most frightening
of images” recalls eugenics and Third Reich mentalities, is the image of the disabled
person as better off dead. (Nelson, 1994). Media examples are found in three 1980’s
dramas; the movie. Whose Life Is it. Anvwav?. the made-for-television, “An Act of Love,”
and the play Nevis Mountain Dew. All of the plots suggest assisted suicide as a potential
alternative to a life with a disability. The fifth image is the disabled person as maladjusted-
his/her own worst enemy. The common scenario is an able-bodied person redirecting the
attitudes of a person with a disability towards success. One more image is the disabled
person as a burden. This dehumanizing image often exists to demonstrate the virtue of the
caregiver, as in Clara doe in Heidi or Tiny Tim in The Christmas Carol. Finally is the
image of the disabled person as unable to live a successful life. People with disabilities are
rarely seen in film unless they serve a dramatic purpose, unless it’s about them, it’s
without them (Nelson, 1994).
“The Cripple in Literature” asks readers to consider how images of disease and
disability “create society’s conception of the cripple and the cripple’s conception of
himself’ (Kriegal, 1987, p. 33) rather than the artist’s personal impressions of the
experience of being wounded. He adds images of the survivor cripple, and the realistic
cripple to the list of stereotypes. The realistic cripple refers to a character who has
incorporated disability into an overall sense of self, like Laura in Tennessee Williams’ The
Glass Menagerie. The survivor cripple triumphs not over misfortune but against it by
outlasting the effects of his wound until they have been incorporated into his way of
dealing with the world,” (p. 33) as in Saul BeUow’s poolroom entrepreneur, William
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Einhom. Others may cry “I am that I am,” but people with disabilities must submit to the
will of others and whimper “I am what you tell me to be” (p. 34).
The search for role models in literature was the youthful quest and impetus for
Deborah Kent’s chapter, “Disabled Women: Portraits in Fiction and Drama” (1987). She
asks how women with disabilities are viewed by writers, why writers use disabled
characters and suggests that an assessment of the disabled woman’s place in literature is a
barometer and predictor of societal perceptions. Character analyses by Charles Dickens,
James Joyce, Walter de la Mare, Tennessee Williams and others result in theories stating
that the disabled woman is severely disadvantaged in creating and maintaining
interpersonal relationships. Other women see her as different and incapable of sharing their
own “overriding interest in men, and men, when not repulsed, are drawn to her to meet
their unhealthy needs” (Kent, 1987, p. 62).
Comic books both shape and reflect popular opinion, say Tim Lees and Sue Ralph
(1995) in the conference presentation, “Case Studies of Physical Disability in Marvel
Comics, 1961-70.” The authors discuss two characters. Dr. Don Blake and Professor
Xavier, a frail, cane-using character who transforms into his alter ego, Thor, by stamping
his cane on the floor. Professor Xavier, the wheelchair-using mentor of the X-Men, calls
to mind the images of mentally-advanced beings with tiny and feeble bodies. The authors
point out that Xavier represents a mind/body dualism and embodies the stereotypical idea
that if one has disability, he/she must compensate with super achievements in the mental
realm. Both men were portrayed as having unnaturally strong moral characters. The
authors question the portrayal of a good man in a wheelchair. They ask why he can’t
have human flaws. They conclude that while the introduction of disabled characters into
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comic books may have raised the profile of disabled people in a superficial sense, it also
perpetrated many harmful stereotypes (p. 9).
Children’s literature, a powerful tool for teaching and helping children to solve
everyday problems, is another potential spot for damaging stereotypical and limiting
images. Children directed messages often malign the disability experience (Saad,1996). In
“traditional fairy tales, there exists a polarization which equates slowness or
unattractivenesg with evil.” Many times they are helpless and needy (Saad, 1996, p.4).
Even in children’s literature the characters must overcome disability through prayer or
hard work: if a child cannot transcend his/her illness, the implication is that they are
lacking in some way. If they cannot rid themselves of disabilities, the characters often gain
acceptance by becoming heroes. Saad (1996) concludes that ‘children’s literature is a
powerful medium affecting readers’ attitudes,” and so it is imperative that its images of
people with disabilities be positive and realistic (p. 5).
The communication of the disability experience through mainstream entertainment,
literature, and teaching tools is society’s method for creating and regenerating faulty and
profoundly limiting perceptions of disability. The influx of contradictory, reality based
narrative into the existing data updates and shifts ways in which the experience is
perceived and ultimately impacts the experiences of disability itself.
After too long a period of silence, “[t]hose who have been objects of others’
reports are now telling their own stories. As they do so, they define the ethic of our times:
an ethic of voicç, aflfording each a right to speak her own truth, in her own words” (Frank,
1995, p. 9). Exploring the essence of disability fi*om the first person vantage, asking the
question, ‘if I am not my body, then what am I?, becomes fodder for ethnographic
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research. Scholars seeking answers have dissected the disability experience, revealing
ways that the experience affects individuals, community and society.
The Bodv Silent chronicles one man’s journey from having a fully functioning body
to having a severely impaired one. Robert Murphy, an anthropology professor at
Columbia University, remarks on the significance of the relationship between paralysis and
the human condition. “The study of paralysis is a splendid arena for viewing this struggle
of the individual against society, for the disabled are not a breed apart but a metaphor for
the human condition” (Murphy, 1990, p. 5). In the pages of his journal, exploring
euthanasia, isolation, the responsibility of wellness and the costs of illness, he repeatedly
asks the question, “what constitutes living”? As Murphy treks into the unknown, he
draws on his training as a researcher to uncover the secrets of a New World. He recounts
positive feedback from an early edition of his book.
The Body Silent did something for the disabled: It told them that the avoidances
and even outright hostility so often manifested toward them by the non-disabled
are not the natural products of their own physical deficits but, rather, expressions
of deficiencies of perspective and character of those who so behave—in short, it is
their problem, not ours (Murphy, 1990, p.vi).
Feminist writers often include perspectives on embracing the rejected body. “Ideas
of transcending the body have been rejected .. . because they are seen to originate from
philosophies and/or religions that devalue the body (especially women’s bodies) and bodily
experience (Wendell, 1996, p. 165). The British scholar, Jenny Morris applauds the shift
from a medical to a social construction of disability, but cautions that there is a
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tendency within the social model of disability to deny the experience of our own
bodies, insisting that our physical differences and restrictionsentirely are socially
created. While environmental barriers and social attitudes are a crucial part of our
experience of disability - and do indeed disable us - to suggest that this is all there
is to it is to deny the personal experience of physical or
intellectual restrictions, of illness, of the fear of dying. A feminist perspective can
help redress this, and in so doing give voice to the experience of both disabled men
and disabled women (Morris, 1991, p. 10).
Women’s accounts of disability often address limitations as the extent to which they are
unable to serve others. Susan Wendell, a professor of women’s studies in British
Columbia, is not surprised that her “greatest psycho-ethical struggle is with guilt”
(Wendell, 1996, p.5). Internalization of negative images is one way that poor self images
are created. Lonsdale (1990) offers four more reasons why women (although men report
similar fears) with disabilities have a difficult time in social situations. The first reason is
her experience of negative reactions fi-om the outside world. The second is her lack of
control over “normal body fimctions. Next is her need to incorporate cold, hard, metallic
appliances into a warm and soft feminine presence. The fourth reason given is fear of
sexual and social rejection ( p. 66).
The importance of understanding the disability experience, not merely on its own
merits as a cultural diversity, but in terms of its relationship to and its effect on
mainstream culture is emphasized by Cahill and Eggleston (1994) in “Managing Emotions
in Public: The Case of Wheelchair Users”. They contend that the wheelchair users’
emotional management, both personal and other-directed, of public displays supports the
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hypothesis that this aspect of hidden public interaction should be studied so that public life
can be more fully understood. Another study by Braitwaithe (1991) also investigated
disabled-ablebodied social interactions. She reports results about communication from
people with disabilities when they perceive ablebodied persons are expecting or
demanding disclosure about their disabilities. One of the important study findings
questioned “the prescription that persons with disabilities shouldalways disclose about
their disability. While disclosure may make ablebodied people more comfortable,
disclosure may not always be advantageous for the disabled person, either relationally or
personally” (p. 267).
Michael Berube’s (1997) article in The Chronicle of Higher Education asks why
disability is not seen as the potentially universal condition that it is. He claims that
“understanding disability as an integral part of the human condition means imagining
ourselves in their places—and that may be too much of a psychological burden for us to
bear” (p. B5). The author, father to a child with Down syndrome, questions the images of
disability and their relationship to real world situations. Berube suggests the inclusion of
disabilities studies in college anthropology, history, and literature courses: “If we bring
those perspectives to bear on the humanities, perhaps we will understand humanity.
Perhaps, too, if we are fortunate, we can help to create a political climate in which all
persons with disabilities are recognized and valued, even if they’re not as charming as
Forrest Gump or as heroic as Billy Bob Thornton’s Karl (from the movie Slingblade)” (p.
B5).
The discipline of Communication studies is another area of disability research.
Thompson’s “The Way We Were,” (1997) asserts that “(d)isability is socially constructed
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as a defining characteristic of an individual” (p. 8). She documents her search for a
discipline that would fully support her own interest in disability studies through special
education, symbolic-interaction sociology, and communication.
Haller (1997) notes that “in the 1990’s little research has focused how local media
can more often and more accurately cover the disability community and disability issues”
(p. 4). She reports that two possible positive media images for people with disabilities are
(1) “the minority group model, in which the disability community is seen as deserving of
civil rights and (2) the consumer model, in which equity in society for people with
disabilities in society is seen as good economic sense” (p. 10). Affirming the power of the
media in the social construction of disability, she implores communication scholars to
focus on “assessing this potential change” (p. 12).
As a disability culture emerged, those living with “biological defects that cannot
be cured and that inhibit, to some extent, their ability to perform certain functions”
(Ingstad, 1995, p. ix) express their own views of society and of themselves. Their rage
against political policies, societal misconceptions and medical model language, all defining,
incorrectly, the disability experience, produced a result greater than each individual
success.
Constructing and Deconstructing Disabilitv: Medical and Social Models
The way that disability is understood is as central to the disability experience as is
the nature of the contracted impairment. Recent years have seen shifts in consciousness
surrounding the epistemological and ontological contexts of disability. Previously,
disability was seen as an individual or medical problem focused on a body that worked (or
didn’t) differently, more weakly, or chronically less able than expected.
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The decision to assign medical meaningsdisability to has had many and varied
consequences for disabled people. One clear benefit has been the medical
treatments that have increased the well-being and vitality of many disabled people,
indeed have saved many people’s lives.. .. Yet, along with these benefits, there
are enormous negative consequences. .. . Briefly, the medicalization of disability
casts human variation as deviance firom the norm, as pathological condition, as
deficit, and, significantly, as an individual burden and personal tragedy. Society, in
agreeing to assign medical meaning disability,to colludes to keep the issue within
the purview of the medical establishment, to keep it a personal matter and “treat”
the condition and the person with the condition rather than “treating” the social
processes and policies that constrict disabled people’s lives (Linton, 1998, p. 11).
Currently, disability is recognized as a social or community problem, the
environmental, social, and political barriers are seen essential determinants of handicap.
Without a conception of disability as a social construct, explanations of the results
of modem “disability legislation” are incomplete. What is not accounted for is the
fact that laws that deal with handicapped people reflect not only the political
problems posed by conflicting interest groups, but also the views that biological
deficiency confers social deficiency... . Useful legislative evaluations need to take
into account the processes by which people who deviate fi’om accepted physical
norms are devaluated and segregated, and, as a result, disabled (Liachowitz, 1988,
p.l).
The changes have been reflected in social and personal experience, in legislation,
and in language use.
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The present examination of disability has no need for the medical language of
symptoms and diagnostic categories. Disability studies looks to different kinds of
syndromes for its material. The elements of interest here are the linguistic
conventions that structure the meaning assigned to disability and the patterns of
response to disability that emanate from, or are attendant upon, those meanings
There are various consequences of the chosen terminology and variation in
the degree of cpntrol that the named group has over the labeling process (Linton,
1998, p. 8,10).
Recognizing a common community voice. Barton (1996) contends
Disabled people are increasingly involved in challenging stereotypes and
developing an alternative dignified perspective, one which recognizes disability as a
human rights issue. This involves the struggle for choice, social justice and
participation. The voices of disabled people are unmistakably clear on these issues
(p. 13).
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METHODOLOGY
Without having much background information about the social and historical
conditions of disability or without a lengthy discussion of Karl Marx’s theories of
historical materialism, it would stUl be easy to identify a comfortable match between
disability oppression and Marxist theory. Because people with disabilities comprise an
underprivileged class easily defined by their uneasy relationship to the economic
relationships of society, the mode of production, and because Marx names social
inequality as a class-bound, economic fact of society, Marxism places the origination of
disability oppression in that economic dysfunction. The lumpenproletariat, an arguably
suitable description for the class of people with disabilities, is Marx’s name for a class
even more disenfi-anchised than factory workers. This class of people exists outside
socially acceptable modes of production. They are the gypsies, the beggars, and the
unemployed. Of oppressed peoples, they are the most oppressed. To locate
empowerment, though, not instead of, but evolving fi-om, generations of persecution, one
must consider the social implications suggested by Marx’s theory of internal relations.
Marxist theory suggests a world view in which distinct organizations and the
relationships supporting them function independently and interdependently simultaneously.
28
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No process and no relationship exists prior to or independently from any other
process or relationship. Each process exists, literally, as the site of all the other
processes in society. Each process also contributes in part to the existence of all
the other processes in society. This reciprocal, multisided, causality, or mutual
constitution, is what Resnick and Wolff refer to as overdetermination. As each
process is uniquely constituted by its particular determination, it moves in a
complex and contradictory manner. That is to say, as one process changes, so too
do all the others, and therefore any one process is in a constant, non-teleological
flux, overdetermined time and again by the continual, contradictory movement of
its conditions of existence (processes) (Wolff 1996, pp. 145-6).
Accepting this irreducible aggregate as essential, Marx describes a present contained in the
womb of the past, a society with factors as coimected as the sections of any Rube
Goldberg contraption. Empowerment grows from the ashes of Ed Roberts, Helen Keller,
and Wade Blank; from the pens of John Callahan, Nancy Mairs, and Mary Johnson; from
the legislative power of the ADA, the Fair Housing Act and ADAPT; and from the
scholarly efforts of Simi Linton, David Pfieffer, and Paul Longmere.' This chapter not only
explores previous literature describing the use of Marxism to understand the oppression of
disability, but also looks more closely at Marx’s application of the theory of internal
relations (which can be traced to Hegel, Spinoza, and even Aristotle) and its implications
' All these people and organizations represent disability empowerment: Ed Roberts (1939-1995) is called the father of the independent living movement; Helen Keller (1880-1968) was deaf and blind, insisting on equality in a time when either condition guaranteed exclusion; Wade Blank (1940-1993) was an ADAPT founder who recognized a need after his experience as a nursing home attendant; John Callahan is a cartoonist who’s s irreverent humor asks us to look past the expected; Nancy Mairs’ book and essays are personal and poetic observations into the disability experience; Mary Johnson is the editor of The Ragged Edge: Linton, Pfieffer, and Longmere are writers and educators.
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for the disability community. Additionally, it proposes the structure of disability
empowerment and clarifies the purpose of disability press messages.
Oppression
Historically, oppression has been addressed by submerged groups seeking
resolution. Women’s struggles with economic, political and social inequality have
provided insight to the newer civil rights battle of the disability community. Although
some women found the match between Marxism and feminism unsatisfactory for its lack
of gender specificity, “Marxism systematically explained people’s oppression, provided a
“scientific” understanding of historical change, and offered a vision of a truly just society
in which equality, realization of human potential, and the true fulfillment of people’s needs
were ingredient” (Philipson & Hansen, 1990, p. 12). But, in spite of the lack of specific
references to gender issues, there is room within Marxist theoiy to root out the oppression
of women.
Job segregation . . . is the primary mechanism in capitalist society that maintains
the superiority of men over women, because it enforces lower wages for women in
the labor market. Low wages keep women dependent on men because they
encourage women to marry. Married women must perform domestic chores for
their husbands. Men benefit, then, fi-om both higher wages and the domestic
division of labor (Hartmann, 1976, p. 148).
Just as the women’s movement did, the disability rights movement recognizes the
value of utilizing Marxist theory as an appropriate structure for understanding conditions
of inequality. Disability studies scholars, many of them British, have placed the
underpinnings of disability oppression within a Marxian system of economic emphasis.
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Bames (1997) names two possible explanations for the phenomena of negative public
attitudes towards people with disabilities.
The first, and the older of the two, suggests that cultural perceptions of
impairment are shaped by deep rooted psychological fears of the abnormal and the
unknown. The second, explains disabled people’s oppression in term of material
considerations such as the economy and the way that it is organised or what is
sometimes termed the mode o f production (p. 2).
Bames identifies disability oppression as a product of industrial capitalism by recognizing
how the politicization and medicalization of disability affects perceptions. Since people
with disabilities are often excluded fi-om systems of commodity production and
distribution, they are incorporated into a second medically and politically based system
based on perception of need. These systems are covertly designed to keep the
underprivileged in an unemployed state so that others can maintain employment. Bames
(1997) cites a 1966 study which claims that “because of the centrality of work in westem
culture [people with disabilities] are viewed as useless since they are considered not able
to contribute to the economic good o f the community” (p. 5). Bames concludes by
suggesting that changes in the value systems within westem society must precede the full
inclusion of disabled people into mainstream society.
A related study explores the implications of the disabled person’s nonproductivity.
The findings show that
the ability to labour in some socially recognized sense still seems a requirement of
fiiU membership of a future good society based upon Marxist theory.. . . It is hard
to see how despite all efforts by a benign social stmcture an albeit small group of
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impaired people could achieve full social integration. Following Marxist theory . ..
some impaired lives cannot. . . be truly social, since the individual is deprived of
the possibility of those satisfactions and that social membership to which her
humanity entitles her, and which only work can provide. . .. There is then for
Marxism an identity o f who you are with the work you do which transcends
capitalism and socialism into the concrete utopia of the future to constitute key
element of humanity, and a key need of human beings in all eras (Abberly, 1998, p.
187).
Oliver (1996) asserts that Marx can be essential to an ontological understanding of
disability. He suggests the nature of the connection between work, work relationships and
disability images. Since
all phenomena (including social categories) are produced by the economic and
social forces of capitalism, the forms in which they are produced are ultimately
dependent upon their relationship to the economy ( Marx, 1913). Hence, the
economy, through both the operation of the labour market, and the social
organisation of work, plays a key role in determining societal responses . . . to
disability.. . (p. 131, 132).
In an earlier work. The Politics of Disablement. Oliver (1990) devotes a chapter,
“Disability and the Rise of Capitalism,” to a discussion of conditions and contributing
economic factors of the disability experience. He claims that “a framework derived from
historical materialism does. .. add to our understanding of what happened to disabled
people with the coming of industrial society” (p.26). The author states that “historical
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materialism is not just about placing social relationships within a historical setting. It also
attempts to provide an evolutionary perspective on the whole of human history” (p.27).
Oliver turns his discussion to disability empowerment by referencing Marx’s views
of society to support his own theory that man is a totally social being and without society
he does not exist. He claims that empowerment is “a collective process on which the
powerless embark as part of the struggle to resist the oppression of others, as part of their
demands to be ipcluded, and/or to articulate their own views of the world” (1996, p. 147).
Oliver names components of the empowerment transformation as
the rise in the number of organizations controlled by and for disabled people, the
number of groups still emerging to represent the community, the challenge to
mainstream social perceptions of disability as personal tragedy, and the affirmation
of positive images of disability through the development of a politics of personal
identity (p. 152).
Supporting his claim of Marx’s belief in the unity of human consciousness, the author
offers the following quote from Marx:
Though man is a unique individual - and it is just his particularity which makes him
an individual, a really individual social being - he is equally the whole, the
subjective existence of society as thought and experienced. He exists in reality, as
the representation and real mind of social existence, and as the sum of human
manifestation of life (p. 155).
Taken in conjunction with the claim of unity among man, Marx’s concept of the
interdependent nature of social institutions explains the rise in disability empowerment
over the past ten years since the passage of the ADA. Marx’s theory of internal relations
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suggests that no one system (family, law, education, ideological representation [mass
media], or cultural phenomena) is independent of the rest. But, instead, each is nudged by
the other’s movement. If human progress and institutional change are intimately
connected, then it follows that the separate, progressive movements combine to create
something new in human consciousness. Increased awareness results from changes to
legislation (the ADA), health care practices, (home care as a viable alternative to
institutionalization), activist organizations (ADAPT and disability-managed Centers for
Independent Living), educational mainstreaming and the legitimatization of disability
studies programs. Increased awareness, enables, or perhaps, forces the existence of
empowerment.
Internal Relations And Empowerment
Philosophers since the Greek Parmenides have suggested a theory of internal
relations or holism to postulate the nature of existence. Its prominence in the modem
period, though, can be attributed to Spinoza.
Spinoza’s own version of this philosophy is constructed upon Aristotle’s
definition of “substance” as that which is capable of independent existence. Since
only nature taken as a whole is capable of independent existence, it is, according to
this view, the sole substance. It is such a unified nature which Spinoza labels
‘God’. . . . Leibniz, on the other hand, puts his emphasis on the parts and devotes
little attention to the whole he sees reflected in each.. . . Coming a century later,
Hegel was perhaps the first to work through the main implications of the
philosophy of internal relations and to construct in some detail the total system
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which it implied. In this he was aided . . . by the character of the impasse
bequeathed to him by his immediate predecessor, Kant (Oilman, p. 30-31).
Essentially, the theory explains an interconnection between apparently unrelated
concepts and occurrences.
The problem of internal relations . .. may be put very simply. Let us say that A is
related to B. If the absence of that relation would leave A as it was, the relation is
external. If, when, the relation was absent, A would be different, or would cease to
be, the relation is internal (Blanchard, 1989, p.3).
Blanchard goes on to name four characteristics of internal relations. He states first that
each individual factor will “overlap with other members of the whole to which they
belong.. . . Secondly, terms that are internally related must stand in a continuum” (p. 12).
A continuum usually has a spatial relationship, but not necessarily in terms of an internal
relations theory, so that even non touching daisies in a field of daisies could be be
considered to be internally related. Blanchard continues, “[tjhirdly, between the terms
related in the continuum there must be difference of degree... [as are] the system of
colors displayed in the spectrum . . . [and] [fourthly internal relations cannot be dealt with
by formal logic” (p. 12-13).
Marx And Internal Relations
Understanding Marx’s use of this theory to explain an economic base and social
superstructure as social praxis and not merely as an affirmation of a finance-driven
universe, the implications of unity in seemingly unrelated events, social movements, and
man’s behaviors is profound.
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In other words, when Marx says “The mode of production of material life
determines the social, political, and intellectual process in general,” we must try to
understand this claim in a way that allows the latter group of factors to vitally
affect the mode of production, and in a way that removes the automatic
dependence of the social superstructure on the economic base. We must do this,
because this is how Marx used his theories in practise (Oilman, 1976, p.9).
The way thqt each factor relates to the others is as an entity, which, even though
independent, can not be considered in isolation.
The ties between [the social relations] are contingent rather than necessary; they
could be something very different without affecting the vital character of the
factors involved. .. such relations are internal to each factor (they are ontological
relations), so that when an important one alters, the fector itself alters; it becomes
something else (Oilman, 1976, p. 15)
Not only are different social factors intimately connected to each other, but fectors are
united through time. “To introduce the temporal dimension . . . we need only view each
social factor as internally related to its own past and future forms, as well as to the past
and future forms of surrounding factors.... Tomorrow is today extended (Oilman,
1976, p. 18). Marx claims that man
does not see how the sensuous world around him is, not a thing given direct from
all eternity, ever the same, but the product of industry and of the state of society;
and, indeed, in the sense that it is an historical product, the result of the activity if a
whole succession of generations, each standing on the shoulders of the preceding
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one, developing its industry and its intercourse, modifying its social organization
according to the changed needs. (Marx & Engels, 1846, p.35)
The ethereal and ubiquitous character of internal relations exists to connect
seemingly unrelated factors and events into something new. Legislation, ethnography, and
the creation of human rights and service organizations exist together through time and
individual intent: “Thus, the book before me expresses and therefore .. .relationally
contains everything from the fact that there is a light on in my room to the social practice
and institutions of my society that made this particular work possible” (Oilman, 1976,
p27). These events, then, coexist to create community awareness. That awareness is the
state of mind leading to revolution.
When people speak of ideas that revolutionize society, they do but express the
fact, that within the old society, the elements of a new one have been created, and
that the dissolution of the old ideas keeps even pace with the dissolution of
conditions of existence. (Marx & Engels, 1847, p. 174)
The awareness of imposed oppression inspires social and political change. “ [0]nly when
[man] has recognized and organized his own powerssocial as powers so that social force
is no longer separated from him aspolitical power, only then is human emancipation
complete” (Marx, 1843, p. 21). This revolution is an ideological one. Empowerment
equals knowledge of equality. As the wheelchair bumper sticker demands: “To go where
everyone has gone before”.
Empowerment And The Disability Press
The images and rhetoric of the disability press characterize the disability
experience as it is and not as it is believed to be through oppressive societal filters.
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Clusters of concepts are identified by naming the major issues of the disability community:
fi-eedom, deinstitutionalization, and equality. These concepts tell the story of reaction to a
pervasive oppression.
There are. Nelson (1996) claims, five primary needs of the disability community
that are only satisfied by the internal press: (I) The press gives recognition to the salience
of disability issues; (2) It sets the standard for sensitivity in covering disability issues; (3) It
provides coverage that is easily received by the target group; (4) It can provide
community members with a sense of identity; (5)It is a forum and a rallying point in
support of civil action activities (p. 6).
Other oppressed minorities have used an internal press to spread their message and
unite their members.
What allowed socialist-feminist ideas to spread across the country as they did was
an underground circulation of papers, articles, and pamphlets that were
mimeographed or printed at the author’s expense or as a project of a socialist-
feminist group or organization (Hansen & Philipson, 1990, p. 10).
Sometimes those messages are in the form of movement rhetoric, visual art, or fi-om
community-driven press. “ These organs provided an identity to their movements and a
core rallying point for their adherents” (Nelson, 1996, p. 7).
Two unrelated, yet relevant, studies set precedent for the way that the current
exploration addresses media images in relationship to group empowerment. Foss (1996)
studies women’s empowerment by focusing on “the process by which women come to see
their symbols, rituals, and regular practices—the content of their experiences that tends to
be overlooked the [dominant] worldview—as legitimate” ( p. 205). She examines visual
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art for the “discursive and nondiscursive data of words, colors, lines, textures, and
images—it may reveal strategies that would not be apparent in a work of discursive
rhetoric alone (p. 206). By noticing the qualities of individual sections and general
characteristics of a room-sized work of art, she recognizes the uniquely feminine
perspective of the work. The author claims that
[ajnalysis of The Dinner Party (the artwork) reveals three primary strategies used
in the work as a means to empower and legitimize women’s authentic voice: (a)
The work is independent from male-created reality; (b) it creates new standards for
evaluation of its own rhetoric; and (c) women are clearly labeled as agents (p.211).
The author claims that with the predomination of female imagery and the lack of
reference to anything male the work “defines women’s culture as derived from women’s
positive experiences rather than in opposition to men’s culture (Foss, 1996, p. 211). The
artwork does for the women’s community what the disability press does for its
community: it presents an alternative vision on its own terms. Foss (1996) recognizes
another value of submerged groups discovering and legitimizing their voice. She claims
they make possible the development of generative theory, displacing stereotype and asking
the viewer to question accepted practices and beliefs. She suggests that “[w]hen we
develop generative theory, as the study of submerged rhetoric encourages, we will have
the satisfaction of knowing that we have not necessarily or unjustly constructed our
inquiry by neglecting alternative views of understanding” ( p. 219).
The rhetoric of minority communities can be analyzed for information about the
stages of growth of the attendant social movement. The second study recognizes how
dominant rhetorical concepts capture and direct internal sentiment. Darcey (1991) tracks
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the emergence of gay pride as a social movement by defining catalytic events that divide
his area of study into conceptually distinct eras. He also names the dominant value appeals
fi-om each of the rhetorical periods he examines. Unity, work, determination, and strength,
achievement, truthfulness, justice, safety and security, and tolerance are the categories he
names. The Defending Fragile Achievements era, the Fortifying Against a Conservative
Tide era and finally the AIDS—Battling the Hydra era are examples of names he gives to
the stages of the gay pride movement (Darcey, 1991).
Groups existing outside society’s mainstream are, nonetheless, subject to
pressures of the dominant group’s images. Recognizing those images as conceived, rather
than natural, is a step towards empowerment. The way that people with disabilities appear,
to themselves and in their circles of existence is influenced by those imposed images. The
dominating opinions generated by years of misrepresentation are absolutely unavoidable.
“Hegemony is dijSuse and appears everywhere as natural. It (re)enforces domination not
only through the (armed) state but also throughout society. The impulses and impressions,
beliefs and values, standards and manners are projected more like sunlight” (Charlton,
1998, p.31). A crucial concept of oppression, according to Marx (1846), is the way in
which the ruling class controls the ideas of the times.
In every epoch the ideas of the ruling class are the ruling ideas, that is, the class
that is the ruling material power of society is at the same time the ruling
intellectual power. The ruling ideas are nothing more than the ideal expression of
the dominant material relationships grasped as ideas, hence of the relationships
which make the one class the ruling one and therefore the ideas of its domination
(p. 89).
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Berger (1982) claims that “[t]he ruling class, according to this theory, propagates an
ideology that justifies its status and makes it difficult for the ordinary people to recognize
that they are bejng exploited and victimized... . The ideas people have are the ideas the
ruling class wants people to have” (p. 50).
The mass media broadcasts the images that serves the purpose of the dominant
power, “it [mass media] still performs [the] job of distracting people fi-om the realities of
our society and of “clouding their minds” with ideas that the ruling class wishes them to
have (p. 54). Alternatively, group media represents self-defined reality. Empowering
images and rhetoric in the disability press exist as counter attacks to false images and
mistaken identities.
Berger (1982) claims that “Marxist thought is one of the most powerful and
suggestive ways available to the media analyst for analyzing society and its institutions”
(p. 44). He suggests five areas of inspection for traditional Marxist analysis of the media.
This study individualizes those areas and suggests three questions be addressed:
(1) What social, political and economic arrangements characterize the disability
community?
(2) Who owns, controls, and operates the publications?
(3) Which concepts and values are being forwarded by the press?
This study wUl look at the categories that define resistance to stereotypical
images propagafed about people with disabilities. These categories; unity, strength,
independence and fi-eedom and sexuality, defy the limiting images of people with
disabilities as pitiable, childlike, helpless and asexual. By inspecting four covers and four
cover stories each of Mainstream. New Mobility. Ragged Edge and Mouth Magazines it
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can be determined what the messages of empowerment are. The effects of empowering
messages can be seen in rising employment rates, increased earnings, and increased
community involvement by people with disabilities. “[M]arxist media analysis [has] a great
deal of appeal—especially to people with a strong sense of social justice and desires for a
more egalitarian , more humane world” (Berger, 1982, p. 64). Using Marxism as a
structure to understand oppression and as a canopy to explain empowerment, this paper’s
methodology is appropriate for a community presenting humanitarian value and right
action as the primary appeals for equality.
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ANALYSIS
Empowerment in The Disability Press
The Random House Webster’s College Dictionarvn991) provides two definitions for
the verb ‘empower’: 1. to give official or legal power or authority to. 2. to endow with an
ability; enable (p. 438). Roget’s Thesaurus (1992) lists four synonyms for the noun
‘empowerment’: enablement, investment, enfi-anchisement, and endowment (p. 19). Feminine
scholarship recognizes that feminism or feminine empowerment
occurs as and when women, individually and together, hesitantly and rampantly,
joyously and with deep sorrow, come to see our lives differently and to reject
externally imposed fixâmes of reference for understanding these lives, instead beginning
the slow process of constructing our own ways o f seeing them, understanding them,
and living them. For us, the insistence on the deeply political nature of everyday life
and on seeing political change as personal change, is quite simply, feminism (Stanley &
Wise, 1983, p. 192).
Over a century ago, W. E. DuBois (1950) envisioned integration as the Black
community’s path to social equality. He believed that “unless a human being is going to have
all human rights, including not only work, but fiiendship, and if mutually desired, marriage and
children, unless these avenues are open and fi'ee, there cap be no real equality and no cultural
43
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integration” (p.220). The disability community is in the process of defining empowerment in
its own terms. The messages in disability press may clarify how this sea change will
materialize.
In order to analyze the messages of the disability press, this study targets four issues
fi’om each of four magazines. Selections are fi-om the 1997-98 issues of Mouth ('MOI.
Mainstream CMAI. New Mobility (NM). and Ragged Edge fRET In the case of Ragged Edge
and Mouth, the four issues represent a full year’s volume. New Mobility and Mainstream are
monthlies. The feature stories are classified as personal or political and then subdivided into
one of three subcategories based on the most fi-equently appearing themes. Finally, selected
stories and covers are individually analyzed.
Each of these publications, written by and for the people of the disability community,
expresses the disability experience uniquely through the images they present and the
accompanying rhetoric. Both Mouth and New Mobility Magazines began publishing the year
that the Americans with Disabilities Act (ADA) passed in 1990. But by that time. The
Disability Rag, precursor of the Ragged Edge, had been in print for ten years. The Disability
Rag modified its rabble-rousing focus, changed names and transformed into The Ragged Edge
in 1997. Mainstream began publishing in 1988 and released its last issue in December, 1998.
Presently, Mouth: Voice of the Disability Nation plays the role of community
conscience, with an unrelenting, demanding and angry voice. The Ragged Edge: The
Disability Experience in America has become an opinion journal, similar to Mouth, but
features the fiction and poetry of writers with disabilities. Mainstream: Magazine of the Able-
Disabled and New Mobility: Disability Culture and Lifestyle, cover news and current affairs,
with an emphasis on lifestyle. While Ragged Edge and Mouth are available by subscription
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only, have no ads and are printed on plain paper. Mainstream’s and New Mobility’s
circulations number more than 20,000 including promotional subscriptions, advertisements
and glossy, full color formats.
Advertising significantly affects each magazine’s content. Two journals. New Mobility
and Mainstream, capitalize on advertising income by producing mainstream quality products.
They are attractively packaged, highly circulated, and represent a veritable but not angry
awareness of disability. The other two. Ragged Edge and Mouth, present a dissatisfied,
rousing, and in-your-face glimpse of the disability experience. Although each of the magazines
offers both social and political views of oppression and inequality, the use of advertising by
Mainstream and New Mobility necessarily softens the message and the hard, political edge
offered by Ragged Edge and Mouth. According to Berger:
One thing that advertising does is to divert people’s attention fi-om social and political
concerns into narcissistic and private concerns. The immediate mission is to sell goods;
the long-range mission is to maintain the class system. In order to sell goods,
advertising has to change attitudes, lifestyles, habits, customs, and preferences while at
the same time maintaining the economic system that benefits fi^om these changes.
(1982, p. 58).
All four magazines of the disability press ask readers to think alternatively. Mouth and
Ragged Edge make several statements by choosing alternative funding. These quarterlies
“transform the rhetoric of revolution into the advocacy of [a] specific cause” (Heartney, 1996,
p. 7). They not only retain editorial fi-eedom, but demonstrate community cohesion by
soliciting funds fi-om subscribers. Advertisements appearing in New Mobüitv and Mainstream
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are relevant, respectful, and occasionally controversial' (NM 8/96, 10/96). Still, they sell a
belief system along with the wheelchair. Using persuasion techniques, advertising’s aim is
intentional. Berger says, “advertising leads people to . . . separate themselves from one
another, it imposes upon them a collective form of taste” (p. 5 6). Ads may respect a disabled
consumer’s physical status, yet insult her feminist awareness.^ Alternative, controversial, and
diverse, the disability press exposes its readers to information that creates awareness,
promoting empowerment.
The Messages
The messages of the press demand equality, independence, and suggest new concepts
of disability. Equality of people with disabilities is a state existing, at times, only in the ideal
and available only as glimpsed through unsuccessful attempts to claim what should be human
rights. The stories report what is and describe what should be. The images are provoking and
honest.
After identifying all the titles, two categories were immediately obvious: the personal
(relating to self or group as individuals) and the political (relating to self or group as
community). Each of these categories is further defined by three subdivisions that serve to
clarify focal points. Political subcategories are ones containing articles that address fighting
the system, social equality/ community challenge, and accessibility; personal ones are lifestyle,
equipment, and personal triumph. Highlighting a need for systemic change and collective
awareness, political messages are a call to action and are persuasive in nature. Personal stories
'New Mobility has printed ads of a partially dressed pregnant woman in a wheelchair and a disabled man lying in a bed with an able bodied woman. ^ New Mobility ran an ad that featured a man in a wheelchair cavorting with a stereotypically “sexy” woman. Although the point was that people in wheelchairs can have fun, expressing an alternative concept, the ad design employed anti feminist concepts..
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offer informative, sometimes exemplary accounts about the experience of living with a
disability. The following table sorts the feature stories of selected issues into these six
categories.
Political
Fighting the Svstem
Fighting the system is easily the category with the most entries. There are 28 entries
appearing here, but only 15 titles in lifestyle, the next largest division. The stories describe
existing unfairness and catalog attempts to change the institutions responsible for the
inequality. The language used is confrontive as in the following titles from Mouth: the
September, October, 1997 issue contained the stories “Disability Nation Declares
Independence From Institutions”, “Nursing Home Operators Rush To Prevent Mass Escape
From Their Prisons”, and “The Real War Has Begun-Enlist Here To Fight For Your
Freedom”. The July/August, 1998 issue featured “Prisoners Of Medicaid Demand Freedom”.
“Justice Denied By Workers’ Comp”appeared in the May/June, 1998 issue. The Ragged Edge
also promotes tfie political: as in the May/June 1998 issue, “The National Association of
Home Builders is our number-one enemy”(p. 13), “The Tactics of Survival” (p. 18), and from
July/August, “Universal Design: Still fighting for respect”.
1. [RE] Living In The Past: The National Association Of Home Builders Takes
On All Comers In Its Unrelenting Fight Against Building Homes All Of Us Can Enter
2. [RE] The department ofjustice and us
3. [RE] Some reflections on the ADA
4. [RE] Pro Se? Nothing to it—how to file your own lawsuit without a lawyer
5. [RE] Beyond Sticks ‘n’ Stones
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6. [RE} Satyagraha And Disability Rights
7. [RE] A Billion Of Us By 2000
8. [Mo] Disability Nation Declares Independence From Institutions
9. [Mo] ADAPT Takes Nation’s Capital By Storm
10. [Mo] Gingrich Introduces Mi CASA-The Medicaid Community Attendant
Services Act
11. [Mo] Clinton ADAPT Summit Scheduled For September 10 At The White
House
12. [Mo] NCIL, Self-Advocates, Justice For AH, N.O.W.-AU Unite With
ADAPT
13. [Mo] Nursing Home Operators Rush To Prevent Mass Escape From Their
prisons
14. [Mo] The Real War Has Begun-Enlist Here To Fight For Your Freedom
15. [Mo] The Department: “there’s A Street In Itta Bena CaUed Freedom.
There’s A Town In Mississippi CaUed Liberty. And There’s A Department In Washington
CaUed Justice.”- a saying among civil rights workers in Mississippi, 1964
16. [Mo] De-Coding The DOJ’s Documents
17. [Mo] Justice Denied By Workers’ Comp
18. [Mo] Prisoners Of Medicaid Demand Freedom
19. [Mo] ADAPT Takes Memphis
20. [Mo] NCIL Adapts DC
21. [Mo] Cuomo Surrenders HUD
22. [Mo] A Mother Calls For IDEA Police
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23. [Mo] Let them in: how parents can educate their neighborhood schools
24. [Mo] Let them skip school
25. [Mo] Docs Unmask Managed Care
26. [NM] Homeward Bound - attendant care and Medicaid
27. [NM] International Rights, Wrongs and Remedies
28. [Ma] The Litigators - disability rights
Social Equality/ Community Challenge
The social equality/ community challenge subdivision stories asks readers to pay
attention to issqes that have significant impact on the daily lives and possibilities for the
disability community (Social equality division #s 2, 4, 7, 10). It is notable that Ma has only
one entry in this subdivision. The issues reveal the community’s value concerns: the moral
(#’sl, 2, 3), the legal (#8), the social (# 4, 5, 10, 11).
1. [RE] Not Dead Yet’s Unique Message
2. [RE[ The Bad Baby Blues: Reproductive Technology & The Threat To
Diversity
3. [RE] Guinea pigs don’t get to say no
4. [RE] Commission on civil rights raps media coverage of the ADA
5. [Mo] The Fire That WiU Not Go Out : Hey, Everybody...This Movement Is
Moving!
6. [Mo] Not Dead Yet Crashes Hemlock
7. [Mo] Preventing kids like us
8. [NM] Medical Marijuana
9. [NM] Crip Caste - the disability community's pecking order
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1 G. [NM] The Ultimate Offense - language
11. [NM] Top 10 U.S. Cities
Accessibility
Accessibility is a primary concern for the disability community. This issue is examined
from both political and personal viewpoints. This issue conceivably fits in either the systems
(#2) or social (#1) subdivision, but stands alone in order to demonstrate the scope of the
topic.
1. [Mo] Greyhound: We Will Ride!- Or Will We?
2. [RE] Design for the 21" century starts now
Personal
Lifestyle
These stories address the issues that impact the personal lives of people with
disabilities as individuals. Issues like childhood experience (#11), employment (#1, 2), home
design (#3,10), body and relationship issues for men (#11) and for women (#4, 5) as well as
options for recreation (#6, 7, 12), sports (#8) and practical information (#9). As expected NM
had the largest percentage of entries in this subdivision, or 66%.
1. [NM] Self - Employed
2. [NM] Finding Work
3. [NM] Designing for Freedom redesign your home
4. [NM] Body Image, Self-Esteem, Relationships, Domestic Violence, Feminism
5. [NM] Women's Health - information from a disabled Ob/Gyn
6. [NM] The World Series of Poker
7. [NM] Soap Doc Mitch Longley
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8. [NM] Skiing: Choices Slopes, Sweet Deals
9. [NM] Mac vs. Windows
10. [Ma] Accessible Housing
11. [Ma] Reimagining Manhood
12. [Ma] The gifted gardener
Health/ Equipment
Maneuvering the demands of an imperfectly ftmctioning body is a requirement for
empowerment. Knowing what equipment (#1,2,7) will facilitate comfort or expand personal
effectiveness is essential. The information her ranges from necessary ( #1,7, 8) to whimsical
(#3)
1. [NM] Cushions
2. [NM] Leak Proofing - incontinence
3. [NM] Dogs on Wheels
4. [NM] Standing Chairs
5. [Ma] A question of balance - seating systems
6. [Ma] Cath Controversy
7. [Ma] Cover - woman in wheelchair saying "I'll make that call"
8. [Ma] Days of whine and noses - Braille wine bottles
9. [Ma] Talking communication - services and equipment
Personal Triumph
One of the offending stereotypical misconceptions of disability is that merely
performing everyday tasks is somehow noteworthy because of perceived difficulty. In the
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disability press, stories of personal triumph are told about those who make a difference,
not only in their own lives, but in the lives of those around them (#2, 3, 5, 7).
1 [Mo] Meet Our Homegrown ADA Enforcers
2. [Mo] Billy Golfus Launches Telethon
3. [NM] Marilyn Hamilton
4. [RE} Fiction: Epilepsy Poster Child
5. [Ma] Edge wise guy John Hockenbeny
6. [Ma] Missing Andy
7. [Ma] Transforming her world —Nancy Mairs
8. [Ma] Cover - man in wheelchair on beach - "Inspirational'
Summarv
There were seventy stories offered by the four magazines. The breakdown is as
follows:
Political stories 41 58.6%
Changing the system 28
Social Equality 11
Accessibility 2
Personal stories 29 41.4%
Lifestyle 12
Health/ equipment 9
Personal Triumph 8
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Story Analysis
The articles listed in the political section, almost 59%, draw attention to common threads
of experience that describe condition of disability. Many of the articles in the personal section
also capture common threads, but omit the rhetoric that holds the system responsible for
injustice. Mouth leads all the publications in the number of political articles printed. Unlike the
other issues, there is no blend of personal and political perspectives. Their stories are
exclusively political. Ragged Edge also recommends political thought to their readers: the
November/December, 1998 issue claimed that “books that go beyond the personal into the
political experience of disability are still harder to find than they ought to be” (p. 21). The
stories are alarming as they report injustice and mistreatment. In Guinea pigs don’t get to say
‘no’, Ervin (1998)compares dangerous drug research involving “decisionally incapacitated”
subjects to the 1930's Tuskegee incident, involving black men and syphilis treatment. New
Mobility’s articles are less political in tone and in number than personal and Mainstream’s are
even less so. Barry Corbet, the editor of New Mobility, often includes a political theme m
“Bully Pulpit”, the editor’s column. Mainstream published the last issue in December of 1998
before discontinuing publication.
“ Lifting Liberty”, one of the pages included with political story # 8 “Disability Nation
Declares Independence From Institutions,” is an example of the angry, confrontive style for
which Mouth Magazine is known. Author, Lucy G win, analogizes nursing homes and the
Berlin Wall. She writes about automatic Health Care Financial Administration expenditures,
“Sometimes it takes a year or more to bring one hostage out and help her or help him to
connect with life in the free world. Two million people with disabilities are hostages behind it.
America pays the $70 billion annual ransom without blinking”(Gwin, 1997, p. 14). The
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subtitle of the story, “Enemies of our liberty are wealthy, powerful”, recognizes conflict and
antagonism between a disabled “us” and an indoctrinated “them”. Each paragraph employs
war terminology to state a case. Freedom, captivity, ‘handicaptivity’, exile, liberty, captors,
underdogs, freedom, hostage, and fight are the words telling the story of the MiCasa home
health care bill\ The accompanying photograph shows demonstrators climbing the Berlin
Wall.
The tenor of the Mouth article sharply differs from story No. 8 in the social equality
division, appearing in New Mobilitv Magazine. The subtitle is a question. “A miracle
medication or an invitation to abuse?’ The story supplies personal information about a
marijuana user before it approaches policy change. The story presents two sides of the issue,
even though it clearly defends marijuana use. The Ragged Edge entry, # 14 in the personal
triumph section, “Epilepsy Poster Child”, is a personal recollection of diagnosis and personal
^The Medicaid Community Attendant Services and Supports Act of 1999, MiCASSA, is proposed legislation which, if signed into law, would allow for a national program of home- and community-based services (attendant services) and would encourage development of system change mechanisms for states to move from the institutional bias that now exists to a community based system. Although programs providing attendant servicescurrently exist in many states throughout the nation, funding for them is far less than what is needed. Many persons with disabilities merely requiring assistance with daily life tasks are wrongly institutionalized in nursing homes solely because they are unable to receive attendant services. MiCASSA allows for choice. For the first time people who are eligible for nursing homes will be able to choose to use their Medicaid dollars for Qualified Community-Based Attendant Services, and live in their own home. Doing this will not only provide a better living environment and qualityo f life for many Americans,it will use Jess tax dollars, since the cost of providing a person with in-home attendant services is much less than the cost of a person occupying a bed in a nursing home. MiCASSA makes good sense. It will save money, and it will put an end to the needless admission of people with disabilities to nursing homes, allowing us to live where most people desire to Jive — at home(www.ca- index.html, 1999).
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pain. It is the story of shame and family misunderstanding. Doctors, medicine, and illness are
the “devils” Finally, story #14 “Being Done” from the personal lifestyles division, printed in
Mainstream Magazine, is an excerpt from Leonard Kriegal’s memoir Flving Solo. There are
no expressions of anger, only the poetic constructions recalling wisdom gained through the
pain of polio hot-bath treatments. Kriegal ponders his crippled body and its ability to transport
him through a life where he must “be a man.” He writes, “If I could not admit that life as a
cripple with deipand courage of me, I was already doomed.. . . It was difficult, if not
impossible, to know whether one was up to what disease had done to one’s life”
(Kriegel,1997, p28). Experience for the sake of wisdom gained, pain survived for the value of
courage found, and insight won at the expense of humiliation and alienation are the life
messages conveyed
Cover Analvsis
The four covers, chosen because the content of each was consistent with the majority
of covers from (he issue it represents, are analyzed for the messages they send graphically.
The June/July 1998 MA features a middle-aged woman, wearing glasses and a black T-shirt
with the words ‘SHRINK RESISTANT’ printed in block capital letters. She is smiling at the
camera. The title “Psychiatric Survivors” is to the left of her head and a no smoking sign is a
blurred patch of red off her other shoulder. She stands in front o f a white columned entrance
of a red brick building. Featured story titles, “Wheelchairs and Batteries” and “Artist Frank
Moore” are situated over the magazine banner. The boldness of the printing on her shirt might
imply strength as her stance outside the formidable building might be seen as escape. The term
‘psychiatric survivor’ denotes victory, hard fought, as might her smile. The other stories are
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equipment and personal triumph stories. This issue cover mixes in the political with emphasis
on the personal.
The June 1998 issue of NM pictures a side, rear view of a man seated in a manual
wheelchair, wearing a work shirt, between the foot of a prison cot, a closed. Commode and
the wall shadowed with prison cell bars. His head is bowed, as though he is in thought or
reading. The title to that story, “Disability behind bars: should the ADA. protect prisoners?”,
and the other featured stories , “Affordable, Accessible travel”, “Chat Rooms: A cure for the
blues” and “Basketball at 50: Shooting for the mainstream” hang at the head of the bed. The
question offered by the title indicates softness on this political issue. The man’s posture
suggests defeat or consideration. Other stories fit the lifestyle division.
The May/ June, 1998, issue features a drawing of a two story building, shaded in
blue, with an attic window and white columns, porch and wide steps. The caption reads
LIVING IN THE PAST, with a subtitle. The National Association of Home Builders takes on aU
comers in its unrelenting fight against building homes all of us can enter. In a sidebar, the
featured stories are listed: Superman’s Telethon, Not Dead Yet’s Unique Message, and
Fiction: Epilepsy Poster Child. RE’s bent is more political than either of the other
publications considered. The cover story address system change as do MA’s and NM’s. but
additionally the feature articles tend toward the political, too.
The MO cover, easily the most political of the four, bears a cover story titled
“Disability Nation Declares Independence fi-om Institutions”. The title hangs over a red and
white striped flag with the ADAPT fi-eedom symbol (the traditional handicapped icon with
stick arms stretched overhead breaking fi-ee fi-om restricting chains) in a red field usually filled
with fifty stars. The title, the flag and a blurred picture of a woman in a wheelchair next to the
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liberty bell all are superimposed on the Declaration of Independence. The automatic
connection to national values of liberty and freedom reinforces the inciting language of the
title. The message of freedom as an American privilege, hard won and covetously protected is
inescapable. The title “Put Your Power behind H.R. 2020”, cuts across the top right comer of
the page. All the feature articles are political; “ADAPT Takes Nation’s Capital By Storm”,
“Gingrich Introduces Mi CASA-The Medicaid Community Attendant Services Act”, “Clinton
ADAPT Summit Scheduled For September 10 At The White House”, “NCIL [National
Council on Independent Living], Self-Advocates, Justice For All, N.O.W.-AU Unite With
ADAPT”, “Nursing Home Operators Rush To Prevent Mass Escape From Their Prisons”, and
“The Real War Has Begun-Enlist Here To Fight For Your Freedom”.
Conclusion
Part of the process of empowerment for the disability community must necessarily be
self-knowledge. Only after recognizing where the community has been, and where it is now,
can a future be envisioned. The combination of content and rhetorical analysis presented here
highUghts the sometimes angry, sometimes frustrated, usuaUy alternative positions of the
vastly individual, yet intricately bonded community. Since “these organs provide an identity to
the movement and a core raUying point for . . . adherents” (Nelson, 1996), it serves us to
understand which are the essential issues. The press characterizes the community’s pain as
being inflicted from misunderstanding, standard operating procedure and mainstream
ignorance. The community’s triumph comes through unity, perseverance and wisdom gained
through experience. Knowing that a majority of the messages are poUtical ones, 68% of that
majority a demand for systemic change, it comes as no surprise to discover that empowerment
in the disabUity community focuses on changing systems, often through legislative procedures.
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Whether changing existing systems precedes or replaces changes to social and material
attitudes and practice is unclear.
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. CHAPTER V
Conclusions And Future Study
Political Awareness
The messages of the disability press paint a picture of the disability community.
Although the messages are predominately political ones, covering community issues, there
is ample coverage of the personal concerns of disability. The nature of the personal
messages provides insight into the state of empowerment in the disability community.
Community empowerment begins with the commonality of personal experience. The
personal pieces provide poignant and necessary vantages to a wide range of emotional and
practical glimpses of life challenges confronted and surmounted. The political ones build
on the common^ty discovered through personal revelation. Waging a war with words,
the political articles arouse and incite, seeking to change the status quo. Political
awareness is essential for a community seeking change, as Marx (1845), asserts in the
“German Ideology”:
Furthermore, it follows that every class striving to gain control - even when such
control means t}ie transcendence of the entire old form of society and of control
itself, as is the case with the proletariat - must first win political power in order to
represent its interest in turn as the universal interest, something which the class is
forced to do immediately (p. 120).
59
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The articles that recognize a systemic cause as the root of disability oppression
echo charges of other oppressed groups that “the personal is the political”; women
protesting patriarchy, dissenters decrying imperialism. Blacks rejecting white supremacy
and Socialists fighting systemic causes of hunger and poverty. According to Z, a socialist
magazine described as a community of people concerned about social change:
In each instance we uncovered that “the personal is political,” i.e., the experiences,
feelings, and possibilities of our personal lives were not just a matter of personal
preferences and choices but were limited, molded, and defined by the broader
political and social setting. They feel personal, and their details are personal, but
their broad texture and character, and especially the limits within which these
evolve, are largely systemic. In this sense, the contribution of the New Left was to
say that we suffer a “totality of oppressions,” systemically based, entwined, and all
needing to be eliminated via a revolution” in existing institutions, and the creation
of new liberating ones .
The “personal is political” therefore meant that our personal lives are in
considerable part politically delimited and determined so that improving our
personal experiences meant we must collectively address political relationships and
structures (1997, p. 6-7).
The disability press portrays the community of persons with disabilities as a force
collectively addressing political structures and relationships. Empowerment, for the
community, is necessarily a political process.
The Disabilitv Press and Political Action
There has been no significant change over the past ten years in employment or
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income figures of persons with disabilities. But, in spite of these disappointing indicators,
there is still reason to believe the claim of disability empowerment. There is evidence from
the community press that people with disabilities are more political than ever before.
Increased political awareness signals self-determination, a critical component of an
empowered state. In a community where most standard benchmarks of success like
financial wealth, suitable employment, and independence, may be grossly unattainable,
alternative signposts emerge as substitutes. Individuals, awakening to the recognition that
their personal injustice fits a pattern of injustice, are utilizing legislation, mass
demonstration, and modification of academic curricula in order to seek equality.
Achieving self-determination:
requires not only that persons with disabilities develop inner resources, but also
that society support and respond to them. Self - determination is a lifelong
interplay between the individual and society, in which the individual accepts risk —
taking as a fact of life and in which society, in turn, bases an individual’s worth on
ability, not disability.
Persons with disabilities who want to achieve self — determination
need to learn how they can trust and respect themselves. They also need to learn
to identify their rights and needs and to find the most appropriate ways of
communicating these privileges to others. Most important, people with disabilities
must acquire a sense of political purpose and an understanding of their rights,
responsibilities, and the democratic process (Ward, 1993, p. xvii).
Although reverting to legal action, as some articles suggest, in order to solve
dilemmas can be judged as a drain on social resources and an evasion of responsibility, in
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. 62 this case, the use of the legal system is a sign of increased political awareness and
empowerment. Wallace Hendricks, economist from the University of Illinois, reports on
the rise in private legal action:
I know of no time series analyses that would be able to measure before-after
effects of the ADA. It is certainly true, however, that the ADA is associated with
a huge increase in the number of law suits that are cited in the Daily Labor Report.
Casual empiricism would suggest that suits involving disabilities have moved ahead
of all other kinds of suits against firms. (Hendricks, 1999, p. I).
Another indication of political awareness appearing in the press is mass
demonstration. Recently, ADAPT supporters gathered in Washington, D C. to rally for the
“integration mandate’ of the ADA. On May 12, 1999, “disability advocates and activists
took their outrage to the steps of the Supreme Court. Marchers filed into the street to
wheel and walk the four blocks, and a magnificent wave of people, 4000 strong according
to Supreme Court police, gathered before the Supreme Court to send a message to the
justices that will decide the fate of the ADA integration mandate (Thomas, 1999, p. 1).
One more demonstration of increased awareness, hence empowerment, for the
community is increased attention to disabilities studies programs throughout the country
.The press covers school systems, although there are none covering higher education.
Linton (1998) recognizes the value of these programs:
It was, at one time, seamless. There were no disjunctures between the dominant
cultural narrative of disability and the academic narrative. They supported and
defended each other. But in the past twenty years, as the flaws in the civic
response to disability have been exposed, as changing social structures and
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. 63 legislative victories reassemble that narrative, the academic tale slips further
behind.
Enter disabilities studies: a location and a means to think critically about
disability, a juncture that can serve both academic discourse and social change.
Disabilities studies provides the means to hold academics accountable for the
veracity and the social consequences of their work, just as activism has served to
hold community, the education system, and the legislature accountable for disabled
people’s compromised social position (p. 1-2).
All of the issues representing emerging empowerment are featured in the
magazines representing the community’s interests. Three of the targeted articles discussed
in the previous chapter dealt with changing school (not university) systems, a majority of
the remainder covered ADA legislation and group action protesting the system. One
article instructed readers on methods for filing their own ADA lawsuits. Searching the
pages of the magazines affords a glimpse of where the community has been, where it is,
and its future vision.
Marxism and Empowerment
Marx’s explanation of the relationship between man and money (including capital,
mode of production and labor) illuminates possible causes of oppression for a number of
alienated populations. His theory, simultaneously placing material considerations as both
determinant and factor of a social superstructure, also has explanatory value for the
disability experience. The inexact, but intrinsically enmeshed relationship between base and
superstmcture is mimicked by the relationships between the material, physical, and social
limitations of disability. But, even though his vision of interconnection is an ideal
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explanation for oppression, it also has value for a community beginning to break patterns,
gain awareness, and shift its consciousness: the empowerment process.
The way that social class impacts persons with disabilities is best demonstrated
through an exception to the rule of poverty. A successful, post-injuiy Christopher Reeve
suggests that wealth is an effective anecdote to many of the oppressions of disability.
Although Reeve has demonstrated that disability, wealth, and social prestige need not be
exclusive, his financial capacity for the best equipment, medical support, and family
responsibility may be a primary determinant of the best scenario results. Nonetheless,
injury remains as physical oppression, no matter what the state of material affairs. For
much of the disabled population, though, poverty aggravates and may be responsible for
disability. Conversely, disability is often a primary eterminant of poverty, whether through
unemployment or astronomical expenses.
The interconnected nature of Marx’s universe allows leaps in consciousness,
resulting in awareness shifts resulting in empowerment. Charlton (1998) says
Marxism typically understood consciousness as metaphorical spirals of practice
(experience) and theory (thought) intertwined. These spirals move incrementally,
quantitatively. Consciousness, however, is not a linear progression. At points this
quantitative buildup congeals into a “rupture,” or a qualitative or transformational
leap to another stage of consciousness where another spiral - like phenomenon
begins.... Consciousness is an awareness of oneself and the world. Furthermore,
consciousness has depth, and as one moves through this space one’s perception of
oneself and the world changes.. . . The point is that consciousness cannot be
separated from the real world, from politics and culture (1998, p.28).
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. 65 This change in consciousness is happening in the disability community. Ten years of
telling personal experience, forming political organizations, passing powerful legislation,
and recognizing disabled others as similar has forced such a non-incremental leap.
Through personal practice, mass demonstration, and systemic change, people with
disabilities are affirming their right to exist on an equal plane as others.
Whether or not Marx’s idealized vision of a world where each is equally free to
develop their talents has predictive value for the community is not known. It is possible
that Marx’s communism, the natural evolution of capitalism, would offer a greater place of
equality for people with disabilities. There are certain aspects of communism that would
benefit the class of people with disabilities. Simon (1994) discusses these factors:
Three important features of communist society, as Marx sketched it, also remain
relevant: the rejection of the market as an organizing principal of social relations,
the abolishment of private ownership of means of production, and the nature and
meaning of egalitarianism. Although at the moment socialism appears to the
receding from the political agenda in most places, the question of the market
persists. Is there a viable alternative to the use of the market as an organizing
principal of our economy and more generally, of society?
The idea of an egalitarian society remains relevant. Marx is often taken to
be an enemy of individualism and individual freedom. This is far from the truth. His
vision was of a society in which individuals could for the first time be free to
develop their talents and abilities. But importantly, it was a society in which all
individuals would be equally free to do this.. . . What Marx saw as the true value
was not equality of result but equality of potential, not equality in tension with
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. 66 freedom but equality that could only be realized along side of true freedom for all.
Communism would not be a society of the equal result or equal achievement. But
it would be a society in which differences in achievement would not be the cause
of jealousy, envy, or of unnecessary and harmful barriers to individual
achievement. This is, for sure, a heady and utopian vision. But properly
understanding the sense in which Marx was an egalitarian does give us some
purchase on the ways in which we are not (Simon, p. xxxiv-xxxv).
Future Studies
This study, suggesting proofs and methods of empowerment, also uncovers a shift
in the epistemology of disability. An integrated model of disability incorporates body-
centered (Medical Model) and other-created (Social Model) thinking to transcend both.
Although, in this model, impairment is a defining factor of the disability experience, an
entire spectrum of social structures, including economic ones, are inextricably connected
to the impairment base. A new model of disability, while respecting past and current
thinking, attempts to develop a broader base for the causes of disability oppression. Future
research on the interconnected nature of disability, based on Marxist Theory may expand
modem theories of disability.
The disability press captures from the community and passes on to the community
a combination of personal experience and the community expression of sentiments and
cries for equality. The disability press is the glue of the community. Future research
questions may look at how the disability press impacts mainstream coverage of disability
issues and even how the representations of the disability press are changing mainstream
values. This study might have had additional information about each catalogued title and
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. 67 specific categorizing details.
Changing the way people think about disability is more than a subtle shift in
consciousness, like the ones made upon realization of the absence of an accessible escape
route or an inaccessible ramp construction. Changing societal decisions about disability are
as gentle as fault line shifts in San Andreas. Porter contends that “[t]he lesson . . . is clear:
writing the disabled body will mean that our most basic conceptions of the body will need
to be rewritten” (Porter, 1993, p. xiv). If we rewrite conceptions of the body, we are
necessarily rewriting ourselves. It follows that with new conceptions of self, the society
that holds the self in relation to millions of other selves will change.
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Graduate College University of Nevada, Las Vegas
Cindy Schwartz McCoy
Home Address: 8617 Highland View Avenue Las Vegas, Nevada 89128
Degrees: Bachelor of Arts The University of the State of New York at Albany
Master of Arts University of Santa Monica
Special Honors and Awards: Membership in Lambda Pi Eta The National Communication Association Honor Society
Publications Top Ten U.S. Cities, New Mobility, December, 1997
Thesis Title: The Disability Press: A Wheel Still in Spin
Thesis Examination Committee: Chairperson, Dr. Richard Jensen, Ph.D. Committee Member, Dr. David Henry, Ph.D. Committee Member, Dr. Gage Chapel, Ph.D. Committee Member, Dr. Lawrence Mullen, Ph.D. Graduate Faculty Representative, Dr. Robert Parker, Ph.D.
74
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